# PHENDIMETRAZINE TARTRATE

NDC: 72989-409
Generic name: PHENDIMETRAZINE TARTRATE
Labeler / Manufacturer: Acertis Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20221101

FDA application: NDA018074

## Active ingredients

- PHENDIMETRAZINE TARTRATE: 105 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72989-409"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72989-409
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=162140d3-b833-4633-9759-95821a46a690